QA Equipment Validation Specialist — GMP & Audit Expert

A leading pharmaceutical contract manufacturer seeks a QA Equipment Validation Specialist in Latina, Italy. The role demands validation expertise ensuring compliance with industry standards, with a focus on sterile manufacturing processes. Candidates should have a degree in a scientific discipline and at least 3 years of experience in validation within the pharmaceutical sector. Strong GMP knowledge and excellent communication skills are also essential.

The successful applicant will manage validation documentation and serve as a primary contact during audits.
#J-18808-Ljbffr